Publications by authors named "Amanda Singleton"

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A dual-mechanism antimicrobial peptide with antimutagenic activity targets the replisome and induces cell envelope stress.
Amanda Holstad Singleton, Olaug Elisabeth Torheim Bergum, Jana Scheffold, Synnøve Brandt Ræder, Lilja Brekke Thorfinnsdottir

mSphere· September 2025

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SOS genes are rapidly induced while translesion synthesis polymerase activity is temporally regulated.
Olaug Elisabeth Torheim Bergum, Amanda Holstad Singleton, Lisa Marie Røst, Antoine Bodein, Marie-Pier Scott-Boyer

Front Microbiol· March 2024

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Activation of multiple stress responses in substantially lowers the minimal inhibitory concentration when combining two novel antibiotic drug candidates.
Amanda Holstad Singleton, Olaug Elisabeth Torheim Bergum, Caroline Krogh Søgaard, Lisa Marie Røst, Cecilie Elisabeth Olsen

Front Microbiol· September 2023

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Halogenated Pyrrolopyrimidines with Low MIC on and Synergistic Effects with an Antimicrobial Peptide.
Cecilie Elisabeth Olsen, Fredrik Heen Blindheim, Caroline Krogh Søgaard, Lisa Marie Røst, Amanda Holstad Singleton

Antibiotics (Basel)· July 2022

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Refining the phenotype associated with GNB1 mutations: Clinical data on 18 newly identified patients and review of the literature.
Parisa Hemati, Anya Revah-Politi, Haim Bassan, Slavé Petrovski, Colleen G Bilancia, Amanda Singleton

Am J Med Genet A· November 2018

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Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy.
Hugh J McMillan, Aida Telegrafi, Amanda Singleton, Megan T Cho, Daniel Lelli

Orphanet J Rare Dis· May 2018

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Genetic counseling in industry settings: Opportunities in the era of precision health.
Kirsty McWalter, Megan T Cho, Tara Hart, Rachel Nusbaum, Courtney Sebold, Amanda Singleton

Am J Med Genet C Semin Med Genet· March 2018

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Informed choice in direct-to-consumer genetic testing (DTCGT) websites: a content analysis of benefits, risks, and limitations.
Amanda Singleton, Lori Hamby Erby, Kathryn V Foisie, Kimberly A Kaphingst

J Genet Couns· June 2012

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Clinical features, with video documentation, of the original familial lewy body parkinsonism caused by α-synuclein triplication (Iowa kindred).
Katrina Gwinn, Michael J Devine, Lee-Way Jin, Janel Johnson, Thomas Bird, Amanda Singleton, Andrew Singleton

Mov Disord· September 2011

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Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's disease.
Javier Simon-Sanchez, Melissa Hanson, Amanda Singleton, Dena Hernandez, Aideen McInerney, Andrew B Singleton

Neurosci Lett· July 2005

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Analysis of familial and sporadic restless legs syndrome in age of onset, gender, and severity features.
Melissa Hanson, Melissa Honour, Amanda Singleton, Anthony Crawley, Andrew Singleton

J Neurol· November 2004

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Smell testing is abnormal in 'lubag' or X-linked dystonia-parkinsonism: a pilot study.
Virgilio Gerald H Evidente, Raymund P Esteban, Jose Luis Hernandez, Filipinas F Natividad, Joel Advincula, Amanda Singleton, Andrew Singleton

Parkinsonism Relat Disord· October 2004

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Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2).
Sarah Furtado, Haydeh Payami, Paul J Lockhart, Melissa Hanson, John G Nutt, Andrew A Singleton, Amanda Singleton

Mov Disord· June 2004

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Association between cardiac denervation and parkinsonism caused by alpha-synuclein gene triplication.
Amanda Singleton, Katrina Gwinn-Hardy, Yehonotan Sharabi, Sheng-Ting Li, Courtney Holmes, Andrew Singleton

Brain· April 2004

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Exercise-induced dystonia as a preceding symptom of familial Parkinson's disease.
Michiko K Bruno, Bernard Ravina, Gaetan Garraux, Mark Hallett, Louis Ptacek, Amanda Singleton, Andrew Singleton

Mov Disord· February 2004

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Mutation at the SCA17 locus is not a common cause of parkinsonism.
Dena Hernandez, Melissa Hanson, Amanda Singleton, Katrina Gwinn-Hardy, Jason Freeman, Andrew Singleton

Parkinsonism Relat Disord· August 2003

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Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation.
Stephen Hague, Ekaterina Rogaeva, Dena Hernandez, Cindy Gulick, Amanda Singleton, Andrew Singleton

Ann Neurol· August 2003

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Familial Lewy body diseases.
Katrina Gwinn-Hardy, Amanda Adam Singleton

J Geriatr Psychiatry Neurol· April 2003

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SCA2 may present as levodopa-responsive parkinsonism.
Haydeh Payami, John Nutt, Steven Gancher, Thomas Bird, Melissa Gonzales McNeal, Amanda A Singleton, Andrew B Singleton

Mov Disord· April 2003

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Primary hyperhidrosis--evidence for autosomal dominant inheritance.
Horacio Kaufmann, Daniela Saadia, Charlene Polin, Stephen Hague, Amanda Singleton, Andrew Singleton

Clin Auton Res· April 2003

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